@pcdfoundation

PCD Family Day- Minneapolis 8/23

PCDF NCT RFA

PCD On the Move Scientific Conference 2025

ATS PAR 'Patients and Experts Forum'

Take Action - National Organization for Rare Disorders

Save the date for On the Move Scientific Conference 2025!

PCD Awareness Month- webinar links

Register for Airway Clearance webinar.

Webinar 10/10 Register today!

PCD Awareness Month

An Evening to Ignite the Future

Participation in Clinical Trial Research Survey - Primary Ciliary Dyskinesia (PCD)

Fueling Research In PCD-Webinar Recording

You are invited to join a webinar: Fueling Research in PCD: Updates from the PCDF and ReCode Therapeutics.

Serendipitous Drug Repurposing Through Social Media

PCDF ATS PAR 2024 Patient & Expert Forum

Beat-PCD Newsletter Issue 8

Primary Ciliary Dyskinesia Over Time: What We’re Learning from Natural History Studies

Her Child Was Suffering, and Nobody Could Tell Her Why

White House Rare Disease Forum

PCD Week at ATS

Register today! ReCode Therapeutics Genetics Webinar January 19th

¡Día de la Familia PCD Puerto Rico! PCD Family Day Puerto Rico!

Support Our Work- Donate Now

PCD Awareness Month Education Series: Genetics email 2

Our PCD Stories Matter Story 2

PCD Awareness Month Education Series: Genetics

Our PCD Stories Matter- Story 1

PCD Awareness Month

Resource 1 NIH's Definition of a Clinical Trial | grants.nih.gov

Resource 2 Clinical Trials Glossary - Solving Kids' Cancer

Resource 3 CTG Labs - NCBI

Resource 4: Pipeline - ReCode Therapeutics

Clear the Way PCDF t-shirt shop

Press Release: Parion Biosciences CLEAN PCD Study

Welcome! You are invited to join a webinar: Bronchiectasis in Primary Ciliary Dyskinesia (PCD). After registering, you will receive a confirmation email about joining the webinar.

Beat-PCD survey: 'Patients’ research priorities for primary ciliary dyskinesia'

GDMCC: Investigating the Role of Airway Inflammation in Children with Primary Ciliary Dyskinesia

Welcome! You are invited to join a webinar: Lung Health: Where Are We Going?. After registering, you will receive a confirmation email about joining the webinar.

PCDF ATS PAR 2023 Patient & Expert Forum

What is a rare disease? - Rare Disease Day 2023

PCD Foundation - Helping those affected by Primary Ciliary Dyskinesia

Join us- 20th Anniversary event

PCD Awareness Month ideas

2022 Move 4 A Cure 5-5-5 virtual race 8th annual

Breathe for PCD t-shirts